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Profile of Gaze Dysfunction following Cerebrovascular Accident

Aim. To evaluate the profile of ocular gaze abnormalities occurring following stroke. Methods. Prospective multicentre cohort trial. Standardised referral and investigation protocol including assessment of visual acuity, ocular alignment and motility, visual field, and visual perception. Results. 91...

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Autores principales: Rowe, Fiona J., Wright, David, Brand, Darren, Jackson, Carole, Harrison, Shirley, Maan, Tallat, Scott, Claire, Vogwell, Linda, Peel, Sarah, Akerman, Nicola, Dodridge, Caroline, Howard, Claire, Shipman, Tracey, Sperring, Una, MacDiarmid, Sonia, Freeman, Cicely
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3914228/
https://www.ncbi.nlm.nih.gov/pubmed/24558601
http://dx.doi.org/10.1155/2013/264604
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author Rowe, Fiona J.
Wright, David
Brand, Darren
Jackson, Carole
Harrison, Shirley
Maan, Tallat
Scott, Claire
Vogwell, Linda
Peel, Sarah
Akerman, Nicola
Dodridge, Caroline
Howard, Claire
Shipman, Tracey
Sperring, Una
MacDiarmid, Sonia
Freeman, Cicely
author_facet Rowe, Fiona J.
Wright, David
Brand, Darren
Jackson, Carole
Harrison, Shirley
Maan, Tallat
Scott, Claire
Vogwell, Linda
Peel, Sarah
Akerman, Nicola
Dodridge, Caroline
Howard, Claire
Shipman, Tracey
Sperring, Una
MacDiarmid, Sonia
Freeman, Cicely
author_sort Rowe, Fiona J.
collection PubMed
description Aim. To evaluate the profile of ocular gaze abnormalities occurring following stroke. Methods. Prospective multicentre cohort trial. Standardised referral and investigation protocol including assessment of visual acuity, ocular alignment and motility, visual field, and visual perception. Results. 915 patients recruited: mean age 69.18 years (SD 14.19). 498 patients (54%) were diagnosed with ocular motility abnormalities. 207 patients had gaze abnormalities including impaired gaze holding (46), complete gaze palsy (23), horizontal gaze palsy (16), vertical gaze palsy (17), Parinaud's syndrome (8), INO (20), one and half syndrome (3), saccadic palsy (28), and smooth pursuit palsy (46). These were isolated impairments in 50% of cases and in association with other ocular abnormalities in 50% including impaired convergence, nystagmus, and lid or pupil abnormalities. Areas of brain stroke were frequently the cerebellum, brainstem, and diencephalic areas. Strokes causing gaze dysfunction also involved cortical areas including occipital, parietal, and temporal lobes. Symptoms of diplopia and blurred vision were present in 35%. 37 patients were discharged, 29 referred, and 141 offered review appointments. 107 reviewed patients showed full recovery (4%), partial improvement (66%), and static gaze dysfunction (30%). Conclusions. Gaze dysfunction is common following stroke. Approximately one-third of patients complain of visual symptoms, two thirds show some improvement in ocular motility.
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spelling pubmed-39142282014-02-20 Profile of Gaze Dysfunction following Cerebrovascular Accident Rowe, Fiona J. Wright, David Brand, Darren Jackson, Carole Harrison, Shirley Maan, Tallat Scott, Claire Vogwell, Linda Peel, Sarah Akerman, Nicola Dodridge, Caroline Howard, Claire Shipman, Tracey Sperring, Una MacDiarmid, Sonia Freeman, Cicely ISRN Ophthalmol Research Article Aim. To evaluate the profile of ocular gaze abnormalities occurring following stroke. Methods. Prospective multicentre cohort trial. Standardised referral and investigation protocol including assessment of visual acuity, ocular alignment and motility, visual field, and visual perception. Results. 915 patients recruited: mean age 69.18 years (SD 14.19). 498 patients (54%) were diagnosed with ocular motility abnormalities. 207 patients had gaze abnormalities including impaired gaze holding (46), complete gaze palsy (23), horizontal gaze palsy (16), vertical gaze palsy (17), Parinaud's syndrome (8), INO (20), one and half syndrome (3), saccadic palsy (28), and smooth pursuit palsy (46). These were isolated impairments in 50% of cases and in association with other ocular abnormalities in 50% including impaired convergence, nystagmus, and lid or pupil abnormalities. Areas of brain stroke were frequently the cerebellum, brainstem, and diencephalic areas. Strokes causing gaze dysfunction also involved cortical areas including occipital, parietal, and temporal lobes. Symptoms of diplopia and blurred vision were present in 35%. 37 patients were discharged, 29 referred, and 141 offered review appointments. 107 reviewed patients showed full recovery (4%), partial improvement (66%), and static gaze dysfunction (30%). Conclusions. Gaze dysfunction is common following stroke. Approximately one-third of patients complain of visual symptoms, two thirds show some improvement in ocular motility. Hindawi Publishing Corporation 2013-10-10 /pmc/articles/PMC3914228/ /pubmed/24558601 http://dx.doi.org/10.1155/2013/264604 Text en Copyright © 2013 Fiona J. Rowe et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Rowe, Fiona J.
Wright, David
Brand, Darren
Jackson, Carole
Harrison, Shirley
Maan, Tallat
Scott, Claire
Vogwell, Linda
Peel, Sarah
Akerman, Nicola
Dodridge, Caroline
Howard, Claire
Shipman, Tracey
Sperring, Una
MacDiarmid, Sonia
Freeman, Cicely
Profile of Gaze Dysfunction following Cerebrovascular Accident
title Profile of Gaze Dysfunction following Cerebrovascular Accident
title_full Profile of Gaze Dysfunction following Cerebrovascular Accident
title_fullStr Profile of Gaze Dysfunction following Cerebrovascular Accident
title_full_unstemmed Profile of Gaze Dysfunction following Cerebrovascular Accident
title_short Profile of Gaze Dysfunction following Cerebrovascular Accident
title_sort profile of gaze dysfunction following cerebrovascular accident
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3914228/
https://www.ncbi.nlm.nih.gov/pubmed/24558601
http://dx.doi.org/10.1155/2013/264604
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